百晓学者学者目录

张月花

副教授、博士生导师、硕士生导师、讲师，西安理工大学

精选作品

期刊论文

2026

开放式创新生态系统下核心企业价值共创专利运营模式研究——基于案例分析的视角

张月花，韩琳，牟嘉怡

《未来与发展》

2025

Does inequality perception affect commercial insurance purchase? Evidence from household survey data in China

Xianjie Chen, Yuehua Zhang, Wei Zhang, Jiashan Li

Applied Economics

DOI

2025

企业专利商业化运营研究脉络、动态与趋势——基于开放式创新与共享经济的视角

张月花，姬永茹，陈燕

《生产力研究》

DOI

2025

Dynamic visualization of endoplasmic reticulum viscosity in living cells with a multirotor-based fluorescent probe.

Yuehua Zhang, Nuo Dong, Shiyu Nan, Huijie Dang, Yuan Cheng, Li-Qing Lu, Mei Wang, Ping-Zhu Zhang, Hua Chen, Chao Wei

Chemical Communications

DOI

2025

A pyridinemalononitrile-based polarity-responsive fluorescent probe for lipid droplet dynamics tracking and nonalcoholic fatty liver disease diagnosis.

Boyu Feng, Hanbing Zhao, Yuan Cheng, Yuehua Zhang, Xuan Ji, Ping-Zhu Zhang, Hua Chen, Chao Wei

Analytica Chimica Acta

DOI

2024

人力资本质量与企业创新绩效：经验证据及影响机制

张月花，杨林，陈燕

《西安电子科技大学学报(社会科学版)》

2023

Optimal Debt and Risk Balancing Behavior of Rural Households in China: Evidence from a Discrete Choice Experiment

Yanling Peng, Li Zhou, Qinwen Wang, Rong Kong, Hong Fu, Yuehua Zhang, Calum G. Turvey

Emerging Markets Finance And Trade，Vol. 590, No. 20

DOI

2023

A simple ratiometric fluorescent probe for two-photon imaging of carbon monoxide in living cells and zebrafish.

Jun-Bin Tang, Ping-Zhu Zhang, Zimeng Li, Yuehua Zhang, Hua Chen, Xiao-Liu Li, Chao Wei

Bioorganic chemistry (Print)

DOI

2023

Electroclinical Features and Long-Term Photosensitivity Outcome in Patients With Photoparoxysmal Response With Epilepsy.

Yue Niu, P. Gong, Xian-Ru Jiao, Zhao Xu, Zongpu Zhou, Yuehua Zhang, J. Qin, Zhi-Xian Yang

Pediatric Neurology

DOI

2023

PACS gene family-related neurological diseases: limited genotypes and diverse phenotypes

Han Zhang, Kai Gao, Shuang Wang, Yuehua Zhang, Zhi-Xian Yang, Ye Wu, Yu-Wu Jiang

World Journal of Pediatrics

DOI

2022

Heterogeneous choice in WTP and WTA for renting land use rights in rural china: Choice experiments from the field

Hong Fu, Yanling Peng, Linyi Zheng, Qi Liu, Li Zhou, Yuehua Zhang, Rong Kong, Calum G. Turvey

Land Use Policy，Vol. 1190

DOI

2022

Genetic and phenotypic spectrum of Chinese patients with epilepsy and photosensitivity

Yue Niu, P. Gong, Xian-Ru Jiao, Zhao Xu, Yuehua Zhang, Zhi-Xian Yang

Frontiers in Neurology

DOI

2022

Correction to: Dravet syndrome-associated mutations in GABRA1, GABRB2 and GABRG2 define the genetic landscape of defects of GABAA receptors

C. C. Hernandez, Xiao-Juan Tian, Ning-Ning Hu, Wang-Zhen Shen, Mackenzie A. Catron, Ying Yang, Jiao-Yang Chen, Yu-Wu Jiang, Yuehua Zhang, R. L. Macdonald

Brain Communications

DOI

2022

A Rare Presentation Characterized by Epileptic Spasms in ALDH7A1, Pyridox(am)ine-5′-Phosphate Oxidase, and PLPBP Deficiency

Xian-Ru Jiao, P. Gong, Yue Niu, Yuehua Zhang, Zhi-Xian Yang

Frontiers in Genetics

DOI

2022

The Clinical Features and Long-Term Follow-Up of Vitamin B6-Responsive Infantile Spasms in a Chinese Cohort

Xian-Ru Jiao, P. Gong, Yue Niu, Zhao Xu, Ye Wu, Yuehua Zhang, Zhi-xiao Yang

Frontiers in Neurology

DOI

2022

SCN2A-Related Epilepsy: The Phenotypic Spectrum, Treatment and Prognosis

Q. Zeng, Ying Yang, J. Duan, X. Niu, Yi Chen, Dan Wang, Jing Zhang, Jiao-Yang Chen, Xiao-Ling Yang, Jinliang Li, Zhi-Xian Yang, Yu-Wu Jiang, Jian-Xiang Liao, Yuehua Zhang

Frontiers in Molecular Neuroscience

DOI

2022

Efficacy of Ketogenic Diet for Infantile Spasms in Chinese Patients With or Without Monogenic Etiology

Jun Wang, Jie Zhang, Ying Yang, Kai Gao, Ye Wu, Yuehua Zhang, Yu-Wu Jiang

Frontiers in Pediatrics

DOI

2022

Phenotypic Spectrum and Prognosis of Epilepsy Patients With GABRG2 Variants

Ying Yang, X. Niu, Miao-Miao Cheng, Q. Zeng, J. Deng, Xiao-Juan Tian, Yi Wang, Jing Yu, Wenli Shi, Wenjuan Wu, Jie-Hui Ma, Yu-Fen Li, Xiao-Ling Yang, Xiao-Li Zhang, Tianming Jia, Zhi-Xian Yang, Jian-Xiang Liao, Yan Sun, Hong Zheng, Suzhen Sun, Dan Sun, Yu-Wu Jiang, Yuehua Zhang

Frontiers in Molecular Neuroscience

DOI

2022

Efficacy of Anti-seizure Medications, Quinidine, and Ketogenic Diet Therapy for KCNT1-Related Epilepsy and Genotype-Efficacy Correlation Analysis

Zehong Lin, T. Sang, Ying Yang, Yuan Wu, Yan Dong, Tao-Yun Ji, Yuehua Zhang, Ye Wu, Kai Gao, Yu-Wu Jiang

Frontiers in Neurology

DOI

2021

The influence of past experience on farmers' preferences for hog insurance products: a natural experiment and choice experiment in China

Qingyin Cai, Yulian Ding, Calum Tuvey, Yuehua Zhang

Geneva Papers On Risk And Insurance-Issues And Practice，Vol. 460, No. 30

DOI

2021

Heterogeneous choice in the demand for agriculture credit in China: results from an in-the-field choice experiment

Rong Kong, Yanling Peng, Nan Meng, Hong Fu, Li Zhou, Yuehua Zhang, Calum Greig Turvey

China Agricultural Economic Review，Vol. 130, No. 20

DOI

2021

Genotype–phenotype correlation of CACNA1A variants in children with epilepsy

X. Niu, Ying Yang, Yi Chen, Miao-Miao Cheng, Ming Liu, Chang-Hong Ding, Xiao-Juan Tian, Zhi-Xian Yang, Yu-Wu Jiang, Yuehua Zhang

Developmental Medicine & Child Neurology

DOI

2021

De Novo Variants in the DYNC1H1 Gene Associated With Infantile Spasms

Hai-Po Yang, P. Gong, Xian-Ru Jiao, Yue Niu, Qiujun Zhou, Yuehua Zhang, Zhi-Xian Yang

Frontiers in Neurology

DOI

2021

Analysis of the Phenotypic Variability as Well as Impact of Early Diagnosis and Treatment in Six Affected Families With ALDH7A1 Deficiency

Xian-Ru Jiao, P. Gong, Ye Wu, Yuehua Zhang, Zhi-Xian Yang

Frontiers in Genetics

DOI

2021

Phenotype of heterozygous variants of dehydrodolichol diphosphate synthase

Xian-Ru Jiao, Yinan Xue, Sai Yang, P. Gong, Yue Niu, Qi Wang, Huiyong Yang, H. Xiong, Yuehua Zhang, Zhi-Xian Yang

Developmental Medicine & Child Neurology

DOI

2021

GABRB3-related epilepsy: novel variants, clinical features and therapeutic implications

Ying Yang, Q. Zeng, Miao-Miao Cheng, X. Niu, Wenshu XiangWei, P. Gong, Wen-Hui Li, Jie-Hui Ma, Xiao-Li Zhang, Xiao-Ling Yang, Zhi-Xian Yang, Dan Sun, Shui-Zhen Zhou, Jian-Xiang Liao, Yu-Wu Jiang, Yuehua Zhang

Journal of Neurology

DOI

2021

RHOBTB2 gene associated epilepsy and paroxysmal movement disorder: two cases report and literature review

X. Niu, Yan Sun, Ying Yang, Miao-Miao Cheng, Q. Tan, J Zhang, Yuehua Zhang

Acta Epileptologica

DOI

2021

Dravet syndrome-associated mutations in GABRA1, GABRB2 and GABRG2 define the genetic landscape of defects of GABAA receptors

C. C. Hernandez, Xiao-Juan Tian, Ning-Ning Hu, Wang-Zhen Shen, Mackenzie A. Catron, Ying Yang, Jiao-Yang Chen, Yu-Wu Jiang, Yuehua Zhang, R. Macdonald

Brain Communications

DOI

2021

The relationship between the characteristics of burst suppression pattern and different etiologies in epilepsy

Hai-Po Yang, P. Gong, Xian-Ru Jiao, Qiujun Zhou, Yuehua Zhang, Yu-Wu Jiang, Zhi-Xian Yang

Scientific Reports

DOI

2021

Genetic Etiologies in Developmental and/or Epileptic Encephalopathy With Electrical Status Epilepticus During Sleep: Cohort Study

P. Gong, J. Xue, Xian-Ru Jiao, Yuehua Zhang, Zhi-Xian Yang

Frontiers in Genetics

DOI

2021

Phenotypes of GNAO1 Variants in a Chinese Cohort

Xiao-Ling Yang, X. Niu, Ying Yang, Miao-Miao Cheng, Jing Zhang, Jiao-Yang Chen, Zhi-Xian Yang, Yuehua Zhang

Frontiers in Neurology

DOI

2021

Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder

Sukhleen Kour, D. Rajan, Tyler R. Fortuna, Eric N. Anderson, C. Ward, Youngha Lee, Sangmoon Lee, Y. Shin, J. Chae, Murim Choi, K. Siquier, Vincent Cantagrel, J. Amiel, E. Stolerman, S. Barnett, M. Cousin, D. Castro, Kimberly McDonald, B. Kirmse, A. Nemeth, D. Rajasundaram, A. Innes, Danielle C Lynch, P. Frosk, A. Collins, M. Gibbons, Michele L. Yang, I. Desguerre, N. Boddaert, C. Gitiaux, S. L. Rydning, K. Selmer, R. Urreizti, A. García-Oguiza, A. N. Osorio, E. Verdura, A. Pujol, Hannah R. McCurry, J. Landers, S. Agnihotri, E. Andriescu, Shade B. Moody, C. Phornphutkul, M. J. Guillen Sacoto, A. Begtrup, H. Houlden, J. Kirschner, D. Schorling, S. Rudnik-Schöneborn, T. Strom, S. Leiz, Kali Juliette, R. Richardson, Ying Yang, Yuehua Zhang, Ming-Hui Wang, Jia Wang, Xiaodong Wang, K. Platzer, S. Donkervoort, C. Bonnemann, M. Wagner, M. Issa, H. Elbendary, Valentina Stanley, R. Maroofian, J. Gleeson, M. Zaki, J. Senderek, U. Pandey

Nature Communications

DOI

2021

Genetic analysis of 20 patients with hypomyelinating leukodystrophy by trio-based whole-exome sequencing

Huifang Yan, Hao-Ran Ji, T. Kubisiak, Ye Wu, Jiang-Xi Xiao, Q. Gu, Yan-Ling Yang, Han Xie, Tao-Yun Ji, Kai Gao, Dong-Xiao Li, H. Xiong, Zhen Shi, Ming Li, Yuehua Zhang, R. Duan, X. Bao, Yu-Wu Jiang, M. Burmeister, Jing-Min Wang

Journal of Human Genetics

DOI

2020

Livestock insurance, moral hazard, and farmers' decisions: a field experiment among hog farms in China

Xudong Rao, Yuehua Zhang

Geneva Papers On Risk And Insurance-Issues And Practice，Vol. 450, No. 10

DOI

2020

战略性新兴产业专利运营效率评价

张月花，李艳，薛平智

《中国科技论坛》

DOI

2020

Missense variants in the N-terminal domain of the A isoform of FHF2/FGF13 cause an X-linked developmental and epileptic encephalopathy.

A. Fry, Christopher Marra, Anna V. Derrick, W. O. Pickrell, Adam T. Higgins, Johann Te Water Naudé, M. Mcclatchey, S. Davies, K. Metcalfe, H. Tan, R. Mohanraj, Shivaram Avula, Denise Williams, L. Brady, R. Mesterman, M. Tarnopolsky, Yuehua Zhang, Ying Yang, Xiaodong Wang, M. Rees, M. Goldfarb, S. Chung

American Journal of Human Genetics

DOI

2020

[Childhood reducing body myopathy caused by FHL1 gene variation in a child].

Cui-Jie Wei, Zhao-Xia Wang, X. Chang, J. Lyu, L. Ge, Yan-Bin Fan, Yuehua Zhang, Hui Xiong

Zhonghua er ke za zhi = Chinese journal of pediatrics

DOI

2020

Phenotypic spectrum of patients with GABRB2 variants: from mild febrile seizures to severe epileptic encephalopathy

Ying Yang, Wenshu XiangWei, Xiao-Li Zhang, Jiang-Xi Xiao, Jiao-Yang Chen, Xiao-Ling Yang, Tianming Jia, Zhi-Xian Yang, Yu-Wu Jiang, Yuehua Zhang

Developmental Medicine & Child Neurology

DOI

2020

Complex Mosaicism of Two Distinct Mutations in a Female Patient With KCNA2-Related Encephalopathy: A Case Report

P. Gong, Xian-Ru Jiao, Yuehua Zhang, Zhi-Xian Yang

Frontiers in Genetics

DOI

2020

Generation of a human iPSC line from an epileptic encephalopathy patient with electrical status epilepticus during sleep carrying KCNA2 (p.P405L) mutation.

P. Gong, Xian-Ru Jiao, Yuehua Zhang, Zhi-Xian Yang

Stem Cell Research

DOI

2020

Clinical phenotype features and genetic etiologies of 38 children with progressive myoclonic epilepsy

Jing Zhang, Ying Yang, X. Niu, Jiao-Yang Chen, Wei Sun, Chang-Hong Ding, Li-Fang Dai, Liping Zhang, Q. Zeng, Yi Chen, Xiao-Juan Tian, Xiao-Ling Yang, Tao-Yun Ji, Zhi-Xian Yang, Yan-Ling Yang, Yu-Wu Jiang, Yuehua Zhang

Acta Epileptologica

DOI

2020

[Clinical and genetic analysis of childhood-onset myoclonus dystonia syndrome caused by SGCE variants].

Xiao-Juan Tian, Chang-Hong Ding, Yuehua Zhang, Li-Fang Dai, Chun-Hong Chen, Jiu-Wei Li, Xu Wang, T. Han, Xiao-Hui Wang, J. Deng

Zhonghua er ke za zhi = Chinese journal of pediatrics

DOI

2020

Analyzing clinical and genetic characteristics of a cohort with multiple congenital anomalies-hypotonia-seizures syndrome (MCAHS)

Xian-Ru Jiao, J. Xue, P. Gong, X. Bao, Ye Wu, Yuehua Zhang, Yu-Wu Jiang, Zhi-Xian Yang

Orphanet Journal of Rare Diseases

DOI

2020

NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns

H. Stamberger, T. Hammer, E. Gardella, D. R. Vlaskamp, B. Bertelsen, S. Mandelstam, I. D. de Lange, Jing Zhang, Candace T. Myers, C. Fenger, Z. Afawi, Edith P. Almanza Fuerte, D. Andrade, Yunus Balcik, B. Ben Zeev, M. Bennett, S. Berkovic, B. Isidor, A. Bouman, E. Brilstra, Ø. L. Busk, Anita G. Cairns, R. Caumes, N. Chatron, R. Dale, C. D. de Geus, P. Edery, Deepak Gill, Jacob Bie Granild-Jensen, Lauren B. Gunderson, B. Gunning, G. Heimer, J. Helle, M. Hildebrand, Georgie Hollingsworth, V. Kharytonov, E. Klee, B. Koeleman, D. Koolen, C. Korff, S. Küry, G. Lesca, D. Lev, R. Leventer, M. Mackay, E. Macke, Meriel E. Mcentagart, S. Mohammad, P. Monin, Martino Montomoli, E. Morava, S. Moutton, Alison M. Muir, E. Parrini, P. Procopis, E. Ranza, Laura Reed, P. Reif, F. Rosenow, M. Rossi, L. Sadleir, Tara R. Sadoway, H. Schelhaas, Amy L. Schneider, K. Shah, R. Shalev, S. Sisodiya, T. Smol, C. Stumpel, K. Stuurman, J. Symonds, F. T. Mau-Them, N. Verbeek, J. Verhoeven, G. Wallace, Keren Yosovich, Y. Zarate, A. Zerem, S. Zuberi, R. Guerrini, H. Mefford, C. Patel, Yuehua Zhang, R. Møller, I. Scheffer

Genetics in Medicine

DOI

2020

[Clinical phenotypes of epilepsy associated with GABRA1 gene variants].

Ying Yang, Yuehua Zhang, Jiao-Yang Chen, Jie-Hui Ma, Dan Sun, Xiao-Ling Yang, Jing Zhang, Yi Chen, Xi-Ru Wu

Zhonghua er ke za zhi = Chinese journal of pediatrics

DOI

2020

CHD2‐related epilepsy: novel mutations and new phenotypes

Jiao-Yang Chen, Jing Zhang, Ai-Jie Liu, Liping Zhang, Hua Li, Q. Zeng, Zhi-Xian Yang, Xiao-Ling Yang, Xi-Ru Wu, Yuehua Zhang

Developmental Medicine & Child Neurology

DOI

2019

Organization, technology and management innovations through acquisition in China's pork value chains: The case of the Smithfield acquisition by Shuanghui

Yuehua Zhang, Xudong Rao, H. Holly Wang

Food Policy，Vol. 83

DOI

2019

新时期西部高新区功能定位转型发展研究

张月花，薛伟贤，李艳

《生产力研究》

DOI

2019

Heterogeneous clinical and functional features of GRIN2D-related developmental and epileptic encephalopathy.

Wenshu XiangWei, V. Kannan, Yu-Chen Xu, Gabrielle J. Kosobucki, A. Schulien, Hirofumi Kusumoto, Christelle Moufawad El Achkar, Subhrajit Bhattacharya, G. Lesca, Sylvie Nguyen, K. Helbig, J. Cuisset, C. Fenger, D. Marjanović, E. Schuler, Ye Wu, X. Bao, Yuehua Zhang, Nina Dirkx, A. Schoonjans, S. Syrbe, S. J. Myers, A. Poduri, E. Aizenman, S. Traynelis, J. Lemke, Hong-Jie Yuan, Yu-Wu Jiang

Brain : a journal of neurology

DOI

2019

Gene mutational analysis in a cohort of Chinese children with unexplained epilepsy: Identification of a new KCND3 phenotype and novel genes causing Dravet syndrome.

Jiaping Wang, Y. Wen, Qing-Ping Zhang, Shujie Yu, Yan Chen, Xi-Ru Wu, Yuehua Zhang, X. Bao

Seizure

DOI

2019

Infantile epilepsy with multifocal myoclonus caused by TBC1D24 mutations.

Jing Zhang, Jiao-Yang Chen, Q. Zeng, Liping Zhang, Xiao-Juan Tian, Xiao-Ling Yang, Zhi-Xian Yang, Ye Wu, Xi-Ru Wu, Yuehua Zhang

Seizure

DOI

2019

Simultaneous quantification of alpha-aminoadipic semialdehyde, piperideine-6-carboxylate, pipecolic acid and alpha-aminoadipic acid in pyridoxine-dependent epilepsy

J. Xue, Junjuan Wang, P. Gong, Min-Han Wu, Wenshuang Yang, Shi-Ju Jiang, Ye Wu, Yu-Wu Jiang, Yuehua Zhang, T. Yuzyuk, Hong Li, Zhi-Xian Yang

Scientific Reports

DOI

2019

Congenital muscular dystrophies in China

L. Ge, Cheng Zhang, Zhao-Xia Wang, S. Chan, Wen-Hua Zhu, Chun-Xi Han, Xiao-Li Zhang, Hong Zheng, Liwen Wu, Bo Jin, Jingli Shan, B. Mao, Jianmin Zhong, Xiaoyin Peng, Ya-Ying Cheng, Jun-Lin Hu, Yan Sun, Jun-Lan Lu, Y. Hua, Sainan Zhu, Cui-Jie Wei, Shuo Wang, H. Jiao, Hai-Po Yang, Xiao-Na Fu, Yan-Bin Fan, X. Chang, Shuang Wang, X. Bao, Yuehua Zhang, Jing-Min Wang, Ye Wu, Yu-Wu Jiang, Yun Yuan, A. Rutkowski, C. Bonnemann, Wei Wei, Xi-Ru Wu, H. Xiong

Clinical Genetics

DOI

2019

[Pathogenic gene variants and clinical phenotype features of 26 children with progressive myoclonic epilepsy].

Jing Zhang, Yuehua Zhang, Jiao-Yang Chen, Tao-Yun Ji, Zhi-Xian Yang, Xiao-Ling Yang, Wei Sun, Liping Zhang, Xi-Ru Wu

Zhonghua er ke za zhi = Chinese journal of pediatrics

DOI

2019

Three cases of progressive myoclonic epilepsy caused by KCNC1 gene mutations and literature review

Jing Zhang, Yuehua Zhang, Jiao-Yang Chen, Ying Yang, Q. Zeng, Xiao-Ling Yang

DOI

2019

ATP1A3 mosaicism in families with alternating hemiplegia of childhood

Xiao-Ling Yang, Xiaoxu Yang, Jiao-Yang Chen, Shupin Li, Q. Zeng, A. Huang, A. Y. Ye, Zhe Yu, Sheng Wang, Yu-Wu Jiang, Xi-Ru Wu, Qixi Wu, Li-Ping Wei, Yuehua Zhang

Clinical Genetics

DOI

2019

[A phenotypic and genetic study on β-propeller protein-associated neurodegeneration].

Wen-Hui Li, Qian Chen, Hua Wang, Yuan-Feng Zhang, Ying Yang, Ai-Jie Liu, Wan-Ting Liu, Xin-Na Ji, Zi-Teng Teng, Yu-Cai Chen, Bing-Bing Wu, Haowei Yang, Yi Wang, Yuehua Zhang, Shui-Zhen Zhou

Zhonghua er ke za zhi = Chinese journal of pediatrics

DOI

2019

The Genetic Landscape of Epilepsy of Infancy with Migrating Focal Seizures

R. Burgess, Shuyu Wang, A. Mctague, Katja E. Boysen, Xiao-Ling Yang, Q. Zeng, K. Myers, Anne M Rochtus, M. Trivisano, Deepak Gill, Candace T. Myers, Heather E. Olson, J. Symonds, Sinéad B. Heavin, Simone Yendle, G. Ronen, P. Andrews, A. McLellan, Christopher J. Burke, K. Howell, M. Hayman, J. L. Freeman, M. Mackay, Mustafa A. Salih, T. Stödberg, Lacey Smith, Christelle Moufawad El Achkar, Harini Chellamani, Timothy W. Yu, K.-W. Shang, Elaine C. Wirrell, M. Mehaffey, Mariacristina Giardino, Zi-Meng Ye, Michael S. Hildebrand, S. Berkovic, Amy L. Schneider, Karen L. Oliver, A. Brunklaus, S. Zuberi, L. Sadleir, N. Specchio, R. Guerrini, C. Marini, Yuehua Zhang, H. Mefford, M. Kurian, A. Poduri, I. Scheffer

Annals of Neurology

DOI

2019

The Effects of a Single Oral Dose of Pyridoxine on Alpha-Aminoadipic Semialdehyde, Piperideine-6-Carboxylate, Pipecolic Acid, and Alpha-Aminoadipic Acid Levels in Pyridoxine-Dependent Epilepsy

Junjuan Wang, J. Xue, P. Gong, Min-Han Wu, Wenshuang Yang, Shi-Ju Jiang, Ye Wu, Yu-Wu Jiang, Yuehua Zhang, T. Yuzyuk, Hong Li, Zhi-Xian Yang

Frontiers in Pediatrics

DOI

2019

Clinical and genetic analysis of Chinese patients with KCNQ2 mutation-induced neonatal/infantile epileptic disorders

Han Xie, Xiaoxuan Qu, Yuehua Zhang, Yu-Jia Zhang, Wei-Jing Kong, Kai Gao, Xiaoyan Liu, Ye Wu, Yan-Ling Yang, Xi-Ru Wu

DOI

2019

Analysis of clinical and electroencephalogram characteristics of ring chromosome 14 syndrome

Zhen Zhang, Xue Jiao, G. Pan, Wu Ye, Yuehua Zhang, Zhi-Xian Yang

DOI

2019

Clinical and genetic features in pyridoxine‐dependent epilepsy: a Chinese cohort study

Xian-Ru Jiao, J. Xue, P. Gong, Ye Wu, Yuehua Zhang, Yu-Wu Jiang, Zhi-Xian Yang

Developmental Medicine & Child Neurology

DOI

2019

Epileptic negative myoclonus restricted to lower limbs in benign childhood focal epilepsy with vertex spikes

P. Gong, J. Xue, P. Qian, Hai-Po Yang, Xiaoyan Liu, Yuehua Zhang, Yu-Wu Jiang, Zhi-Xian Yang

European Journal of Neurology

DOI

2019

Seizure Outcome and Its Prognostic Predictors After Hemispherotomy in Children With Refractory Epilepsy in a Chinese Pediatric Epileptic Center

Tao-Yun Ji, Ming Liu, Shuang Wang, Qing-Zhu Liu, Ye Wu, Yuehua Zhang, X. Bao, Wen Wang, Ruo-Fan Wang, Guo-yuan Yu, Xiaoyan Liu, Li-Xin Cai, Yu-Wu Jiang

Frontiers in Neurology

DOI

2018

Cheating? The Case of Producers' Under-Reporting Behavior in Hog Insurance in China

Yuehua Zhang, Ying Cao, H. Holly Wang

Canadian Journal Of Agricultural Economics-Revue Canadienne D Agroeconomie，Vol. 660, No. 3

DOI

2018

西安自主创新中的知识产权保护模式研究

张月花，薛平智

《生产力研究》

2018

Mosaicism and incomplete penetrance of PCDH19 mutations

Ai-Jie Liu, Xiaoxu Yang, Xiao-Ling Yang, Qixi Wu, Jing Zhang, Dan Sun, Zhi-Xian Yang, Yu-Wu Jiang, Xi-Ru Wu, Li-Ping Wei, Yuehua Zhang

Journal of Medical Genetics

DOI

2018

Genetic (idiopathic) epilepsy with photosensitive seizures includes features of both focal and generalized seizures

J. Xue, P. Gong, Hai-Po Yang, Xiaoyan Liu, Yu-Wu Jiang, Yuehua Zhang, Zhi-Xian Yang

Scientific Reports

DOI

2018

The clinical outcome and neuroimaging of acute encephalopathy after status epilepticus in Dravet syndrome

Xiao-Juan Tian, Jin-Tang Ye, Q. Zeng, Jing Zhang, Xiao-Ling Yang, Ai-Jie Liu, Zhi-Xian Yang, Xiaoyan Liu, Xi-Ru Wu, Yuehua Zhang

Developmental Medicine & Child Neurology

DOI

2018

Clinical efficacy of Flunarizine in treating alternating hemiplegia in children and the influencing factors

Shupin Li, Yuehua Zhang, Xiao-Ling Yang, Ai-Jie Liu, Q. Zeng, Jing Zhang, Yu-Wu Jiang

DOI

2018

ILAE-Klassifikation der Epilepsien: Positionspapier der ILAE-Kommission für Klassifikation und Terminologie

I. Scheffer, S. Berkovic, G. Capovilla, M. Connolly, J. French, L. Guilhoto, E. Hirsch, Satish Jain, G. Mathern, S. Moshé, D. Nordli, E. Perucca, T. Tomson, S. Wiebe, Yuehua Zhang, Sameer M. Zuberi

Zeitschrift für Epileptologie

DOI

2018

[Study of GRIN2A mutation in epilepsy-aphasia spectrum disorders].

P. Qian, Xiao-Ling Yang, Xiaojing Xu, Xiaoyan Liu, Yuehua Zhang, Zhi-Xian Yang

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

DOI

2018

Large De Novo Microdeletion in Epilepsy with Intellectual and Developmental Disabilities, with a Systems Biology Analysis.

Kai Gao, Yu-Jia Zhang, Ling Zhang, Wei-Jing Kong, Han Xie, Jing-Min Wang, Ye Wu, Xi-Ru Wu, Xiaoyan Liu, Yuehua Zhang, Feng Zhang, A. Yu, Yu-Wu Jiang

Advances in neurobiology

DOI

2018

Hypomyelinating disorders in China: The clinical and genetic heterogeneity in 119 patients

Hao-Ran Ji, Dong-Xiao Li, Ye Wu, Quanli Zhang, Q. Gu, Han Xie, Tao-Yun Ji, Hui-Fang Wang, Lu Zhao, Hai-Juan Zhao, Yan-Ling Yang, Hong-Chun Feng, H. Xiong, Jinhua Ji, Zhi-Xian Yang, L. Kou, Ming Li, X. Bao, X. Chang, Yuehua Zhang, Li Li, Hui-Juan Li, Zheng-Ping Niu, Xi-Ru Wu, Jiang-Xi Xiao, Yu-Wu Jiang, Jing-Min Wang

PLoS ONE

DOI

2018

Study on gene mutation in benign familial neonatal epilepsy

Q. Zeng, Yuehua Zhang, Xiao-Ling Yang, Ai-Jie Liu, Jing Zhang

DOI

2018

Clinical characteristics of two cohorts of infantile spasms: response to pyridoxine or topiramate monotherapy

J. Xue, P. Qian, Hui Li, Ye Wu, H. Xiong, Yuehua Zhang, Zhi-Xian Yang

World Journal of Pediatrics

DOI

2018

Identification of Novel ARSA Mutations in Chinese Patients with Metachromatic Leukodystrophy

Li Chen, Huifang Yan, Binbin Cao, Ye Wu, Q. Gu, Jiang-Xi Xiao, Yan-Ling Yang, Hui-Xia Yang, Zhen Shi, Zhi-Xian Yang, H. Pan, X. Chang, Jun-Ya Chen, Yu Sun, Yuehua Zhang, Xi-Ru Wu, Yu-Wu Jiang, Jing-Min Wang

International Journal of Genomics

DOI

2018

Clinical and electroencephalogram features of neuronal ceroid lipofuscinosis

Shu-Min Zhang, X. Chang, Jing Zhang, Yu Huang, Zhi-Xian Yang, Xiaoyan Liu, Jiang-Xi Xiao, Xi-Ru Wu, Yuehua Zhang

DOI

2017

Determinants of agricultural household demand for insurance in China from 2004 to 2007

Chu-Shiu Li, Chwen-Chi Liu, Yuehua Zhang

China Agricultural Economic Review，Vol. 90, No. 40

DOI

2017

Genomic mosaicism in paternal sperm and multiple parental tissues in a Dravet syndrome cohort

Xiaoxu Yang, Ai-Jie Liu, Xiaojing Xu, Xiao-Ling Yang, Q. Zeng, A. Y. Ye, Zhe Yu, Sheng Wang, A. Huang, Xi-Ru Wu, Qixi Wu, Li-Ping Wei, Yuehua Zhang

Scientific Reports

DOI

2017

MosaicHunter: accurate detection of postzygotic single-nucleotide mosaicism through next-generation sequencing of unpaired, trio, and paired samples

A. Huang, Zheng Zhang, A. Y. Ye, Yan-Mei Dou, Linlin Yan, Xiaoxu Yang, Yuehua Zhang, Li-Ping Wei

Nucleic Acids Research

DOI

2017

Genetic analysis of benign familial epilepsies in the first year of life in a Chinese cohort

Q. Zeng, Xiao-Ling Yang, Jing Zhang, Ai-Jie Liu, Zhi-Xian Yang, Xiaoyan Liu, Ye Wu, Xi-Ru Wu, Li-Ping Wei, Yuehua Zhang

Journal of Human Genetics

DOI

2017

Study on the causative genes and analysis of genotypes and phenotypes of Dravet syndrome

Xiao-Juan Tian, Yuehua Zhang, Q. Zeng, Jing Zhang, Ai-Jie Liu, Xiao-Ling Yang, Yu-Wu Jiang

DOI

2017

Identification of novel ATP7A mutations and prenatal diagnosis in Chinese patients with Menkes disease

Binbin Cao, Xiao-Ping Yang, Yinyin Chen, Qiong-Hui Huang, Ye Wu, Q. Gu, Jiang-Xi Xiao, Hui-Xia Yang, H. Pan, Jun-Ya Chen, Yu Sun, Li Ren, Cheng-Feng Zhao, Yan Deng, Yan-Ling Yang, X. Chang, Zhi-Xian Yang, Yuehua Zhang, Zheng-Ping Niu, Ju-li Wang, Xi-Ru Wu, Jing-Min Wang, Yu-Wu Jiang

Metabolic brain disease

DOI

2017

Early childhood myoclonic epilepsy: An independent genetic generalized epilepsy with myoclonic seizures as the main seizure type.

Zhi-Xian Yang, J. Xue, Hui Li, P. Qian, Xiaoyan Liu, Yu-Wu Jiang, Yuehua Zhang

Clinical Neurophysiology

DOI

2017

Study of Pathogenic gene spectrum in benign familial infantile epilepsy

Q. Zeng, Yuehua Zhang, Xiao-Ling Yang, Li-hua Pu, Xiaoli Yu, Xiu-Ju Zhang, Jing Zhang, Ai-Jie Liu, Zhi-Xian Yang, Xiaoyan Liu, Shuang Wang, Ye Wu, Xi-Ru Wu

DOI

2017

Electro-clinical-etiological associations of epilepsia partialis continua in 57 Chinese children.

Hui Li, J. Xue, P. Qian, Yuehua Zhang, X. Bao, Xiaoyan Liu, Zhi-Xian Yang

Brain & development (Tokyo. 1979)

DOI

2017

Novel phenotypes of pyridox(am)ine-5’-phosphate oxidase deficiency and high prevalence of c.445_448del mutation in Chinese patients

J. Xue, X. Chang, Yuehua Zhang, Zhi-Xian Yang

Metabolic brain disease

DOI

2017

Genetic epilepsy with febrile seizures plus

Yuehua Zhang, R. Burgess, Jodie P. Malone, Georgie C. Glubb, K. Helbig, Lata Vadlamudi, S. Kivity, Z. Afawi, A. Bleasel, P. Grattan-Smith, B. Grinton, S. Bellows, D. Vears, J. Damiano, H. Goldberg-Stern, A. Korczyn, L. Dibbens, E. Ruzzo, M. Hildebrand, S. Berkovic, I. Scheffer

Neurology

DOI

2017

Severe infantile-onset developmental and epileptic encephalopathy caused by mutations in autophagy gene WDR45

G. Carvill, Ai-Jie Liu, S. Mandelstam, Amy L. Schneider, Amy Lacroix, M. Zemel, J. Mcmahon, L. Bello-Espinosa, M. Mackay, G. Wallace, M. Waak, Jing Zhang, Xiao-Ling Yang, Stephen Malone, Yuehua Zhang, H. Mefford, I. Scheffer

Epilepsia

DOI

2017

[Study on mosaicism of SCN1A gene mutation in parents of children with Dravet syndrome].

Ai-Jie Liu, Xiao-Ling Yang, Xiaojing Xu, Qixi Wu, Xiao-Juan Tian, Xiaoxu Yang, Xi-Ru Wu, Li-Ping Wei, Yuehua Zhang

Zhonghua er ke za zhi = Chinese journal of pediatrics

DOI

2017

Myoclonic epilepsy in infancy with preceding or concurrent afebrile generalized tonic-clonic seizures in Chinese children.

Zhi-Xian Yang, Hui Li, J. Xue, P. Qian, Xiaoyan Liu, Yuehua Zhang

Brain & development (Tokyo. 1979)

DOI

2017

[Analysis of SCN1A deletions or duplications in patients with Dravet syndrome].

Q. Zeng, Yuehua Zhang, Xiao-Ling Yang, Xiaojing Xu, Jing Zhang, Xiao-Juan Tian, Ai-Jie Liu, Xiaoyan Liu, Yu-Wu Jiang, Xi-Ru Wu

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

DOI

2017

Clinical Features of Refractory Status Epilepticus in Various Conditions

Xue-Feng Wang, Yuehua Zhang, H. Leung

DOI

2017

GRIN2A mutations in epilepsy-aphasia spectrum disorders.

Xiao-Ling Yang, P. Qian, Xiaojing Xu, Xiaoyan Liu, Xi-Ru Wu, Yuehua Zhang, Zhi-Xian Yang

Brain & development (Tokyo. 1979)

DOI

2017

Atonic elements combined or uncombined with epileptic spasms in infantile spasms.

J. Xue, P. Qian, Hui Li, Hai-Po Yang, Xiaoyan Liu, Yuehua Zhang, Zhi-Xian Yang

Clinical Neurophysiology

DOI

2017

ILAE Classification of the Epilepsies Position Paper of the ILAE Commission for Classification and Terminology

I. Scheffer, S. Berkovic, G. Capovilla, Mary B. Connolly, J. French, L. Guilhoto, E. Hirsch, Satish Jain, Gary W. Mathern, S. Moshé, D. Nordli, E. Perucca, T. Tomson, S. Wiebe, Yuehua Zhang, S. Zuberi

Epilepsia

DOI

2016

On the Impact of Agricultural Livestock Microinsurance on Death-Loss, Production and Vaccine Use: Observations from a Quasi-Natural Experiment in China

Yuehua Zhang, Xi Zhu, Calum G. Turvey

Geneva Papers On Risk And Insurance-Issues And Practice，Vol. 410, No. 20

DOI

2016

西安高新技术产业知识产权能力评价与比较分析

张月花，薛平智，杨燕华

《中国科技论坛》

2016

Clinical and molecular genetic analysis of a family with late-onset LAMA2-related muscular dystrophy.

Juan Ding, Dandan Zhao, R. Du, Yuehua Zhang, Hai-Po Yang, Jie-Yu Liu, C. Yan, Feng Zhang, H. Xiong

Brain & development (Tokyo. 1979)

DOI

2016

Phenotype and gene mutation screening in familial Dravet syndrome

Xiao-Juan Tian, Yuehua Zhang, Xiao-Ling Yang, Xiaojing Xu, Ai-Jie Liu, Q. Zeng, Xiaoyan Liu, Zhi-Xian Yang, Yu-Wu Jiang

DOI

2016

Classification of the epilepsies: New concepts for discussion and debate—Special report of the ILAE Classification Task Force of the Commission for Classification and Terminology

I. Scheffer, J. French, E. Hirsch, Satish Jain, G. Mathern, S. Moshé, E. Perucca, T. Tomson, S. Wiebe, Yuehua Zhang, S. Zuberi

Epilepsia Open

DOI

2016

[Genotype and phenotype of female Dravet syndrome with PCDH19 mutations].

Ai-Jie Liu, Yuehua Zhang, Xiaojing Xu, Xiaoxu Yang, Z.-X. Yang, Yan Wu, Xiao-Yan Liu, Yu-Wu Jiang, Xi-Ru Wu

Zhonghua er ke za zhi = Chinese journal of pediatrics

DOI

2016

Clinical features and ATP1A3 gene mutations in alternating hemiplegia of childhood patients with epilepsy

Shupin Li, Yuehua Zhang, Xiao-Ling Yang, Ai-Jie Liu, Zhi-Xian Yang, Xiaoyan Liu, Ye Wu, Shuang Wang, X. Bao, Yu-Wu Jiang

DOI

2016

小児における片麻痺性てんかんの臨床的特徴とATP1A3遺伝子突然変異の研究【JST・京大機械翻訳】

Shupin Li, Yuehua Zhang, Xiao-Ling Yang, Ai-Jie Liu, Zhi-Xian Yang, Xiaoyan Liu, Ye Wu, Shuang Wang, X. Bao, Yu-Wu Jiang, Xi-Ru Wu

2016

Clinical characteristics and genetic analysis of 2 children with pyridox(am)ine-5′-phosphate oxidase deficiency

J. Xue, Zhi-Xian Yang, Yuehua Zhang

DOI

2016

家族性DRAVET症候群家系の臨床表現型特徴と遺伝子変異研究【JST・京大機械翻訳】

Xiao-Juan Tian, Yuehua Zhang, Xiao-Ling Yang, Xiaojing Xu, Ai-Jie Liu, Q. Zeng, Xiaoyan Liu, Zhi-Xian Yang, Yu-Wu Jiang, Xi-Ru Wu

2016

乳児のてんかん発作性局所性発作を伴う臨床と遺伝子突然変異の特徴【JST・京大機械翻訳】

K.-W. Shang, Yuehua Zhang, Xiao-Ling Yang, Ai-Jie Liu, Zhi-Xian Yang, Xiaoyan Liu, Yu-Wu Jiang, Xi-Ru Wu

2016

[Clinical characteristics and prognosis analysis of vitamin B6 responsive infantile spasms].

J. Xue, Zhi-xiao Yang, Ye Wu, H. Xiong, Yuehua Zhang, Xiaoyan Liu

Zhonghua er ke za zhi = Chinese journal of pediatrics

DOI

2016

Clinical and genetic analysis of two Chinese infants with Mabry syndrome.

J. Xue, Hui Li, Yuehua Zhang, Zhi-Xian Yang

Brain & development (Tokyo. 1979)

DOI

2016

GM1ガングリオシド蓄積症6例の臨床および遺伝学的研究【JST・京大機械翻訳】

Hao-Ran Ji, Jiang-Xi Xiao, Dong-Xiao Li, Gai-Mei Li, Ye Wu, Huifang Yan, Yan-Ling Yang, Yuehua Zhang, Yu-Wu Jiang, Jing-Min Wang

2016

臨床症状は典型的でないピリドキシン依存性てんかんの1例【JST・京大機械翻訳】

J. Xue, Zhi-Xian Yang, Shuan-Shuan Wang, Yuehua Zhang

2016

Clinical and molecular genetic analysis of six patients with GM1 gangliosidosis

Hao-Ran Ji, Jiang-Xi Xiao, Dong-Xiao Li, Gai-Mei Li, Ye Wu, Huifang Yan, Yan-Ling Yang, Yuehua Zhang, Yu-Wu Jiang, Jing-Min Wang

DOI

2015

战略性新兴产业知识产权能力研究述评

张月花，薛平智

《生产力研究》

2015

Gene Mutation Analysis in 253 Chinese Children with Unexplained Epilepsy and Intellectual/Developmental Disabilities

Yu-Jia Zhang, Wei-Jing Kong, Yang Gao, Xiaoyan Liu, Kai Gao, Han Xie, Ye Wu, Yuehua Zhang, Jing-Min Wang, Feng Gao, Xi-Ru Wu, Yu-Wu Jiang

PLoS ONE

DOI

2015

SCN8A mutations in Chinese children with early onset epilepsy and intellectual disability

Wei-Jing Kong, Yu-Jia Zhang, Yang Gao, Xiaoyan Liu, Kai Gao, Han Xie, Jing-Min Wang, Ye Wu, Yuehua Zhang, Xi-Ru Wu, Yu-Wu Jiang

Epilepsia

DOI

2015

[Clinical features and PRRT2 gene mutation in paroxysmal kinesigenic dyskinesia].

Xiao-Ling Yang, Yuehua Zhang, Xiaojing Xu, Zhi-Xian Yang, Shuang Wang, Ye Wu, Xi-Ru Wu

Zhonghua er ke za zhi = Chinese journal of pediatrics

DOI

2015

[ATP1A3 gene mutations in patients with alternating hemiplegia of childhood].

Xiao-Ling Yang, Yuehua Zhang, D. Yuan, Xiaojing Xu, Shupin Li, Li-Ping Wei, Ye Wu, H. Xiong, Xiaoyan Liu, X. Bao, Yu-Wu Jiang, Xi-Ru Wu

Zhonghua er ke za zhi = Chinese journal of pediatrics

DOI

2015

humu22819-sup-0001-SuppMat

Xiaojing Xu, Xiao-Xu Yang, Qixi Wu, Ai-Jie Liu, Xiao-Ling Yang, A. Y. Ye, A. Huang, Jiarui Li, Meng Wang, Zheng-Xi Yu, Sheng Wang, Zhichao Zhang, Xi-Ru Wu, Li-Ping Wei, Yuehua Zhang

2015

Inborn errors of metabolism and epilepsy in children

Yuehua Zhang

DOI

2015

[Progress in molecular genetics of benign familial infantile epilepsy].

Xaoling Yang, Yuehua Zhang

Zhonghua er ke za zhi = Chinese journal of pediatrics

2015

[Intermittent convulsions and progressive motor and intelligence regression for 4 years in a 11-year-old girl].

Tao-Yun Ji, Yuehua Zhang, Yu-Wu Jiang

Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics

2015

[Analysis of parental origin of de novo SCN1A mutations in Dravet syndrome].

Hui-Hui Sun, Yuehua Zhang, Xiaojing Xu, Xiaoyan Liu, Xi-Ru Wu

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

DOI

2015

Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of “de novo” SCN1A Mutations in Children with Dravet Syndrome

Xiaojing Xu, Xiaoxu Yang, Qixi Wu, Ai-Jie Liu, Xiao-Ling Yang, A. Y. Ye, A. Huang, Jiarui Li, Meng Wang, Zhe Yu, Sheng Wang, Zhichao Zhang, Xi-Ru Wu, Li-Ping Wei, Yuehua Zhang

Human Mutation

DOI

2014

NIPA2 mutations are correlative with childhood absence epilepsy in the Han Chinese population

Yu-Wu Jiang, Yuehua Zhang, Ping-Ping Zhang, Feng Zhang, Han Xie, P. Chan, Xi-Ru Wu

Human Genetics

DOI

2014

ATP1A3 Mutations and Genotype-Phenotype Correlation of Alternating Hemiplegia of Childhood in Chinese Patients

Xiao-Ling Yang, Hua Gao, Jie Zhang, Xiaojing Xu, Xiaoyan Liu, Xi-Ru Wu, Li-Ping Wei, Yuehua Zhang

PLoS ONE

DOI

2014

[Phenotypes and PRRT2 mutation analysis in families with benign familial infantile epilepsy].

Xiao-Ling Yang, Yuehua Zhang, Xiaojing Xu, Xiaoli Yu, Xiu-Ju Zhang, Zhi-Xian Yang, Shuang Wang, Ye Wu, Xiaoyan Liu, Xi-Ru Wu

Zhonghua er ke za zhi = Chinese journal of pediatrics

DOI

2014

Functional Study of NIPA2 Mutations Identified from the Patients with Childhood Absence Epilepsy

Han Xie, Yuehua Zhang, Ping-Ping Zhang, Jing-Min Wang, Ye Wu, Xi-Ru Wu, T. Netoff, Yu-Wu Jiang

PLoS ONE

DOI

2014

Early clinical features of Dravet syndrome with SCN1A mutation

Xiaojing Xu, Yuehua Zhang, Hui-Hui Sun, Xiaoyan Liu, Xiao-Ling Yang, H. Xiong, X. Bao, Shuang Wang, Yu-Wu Jiang, Zhi-xiao Yang, Ye Wu

DOI

2014

Low intracellular magnesium enhances the excitability of thalamocortical network and generates epileptic discharges

Han Xie, Yuehua Zhang, Ping-Ping Zhang, Jing-Min Wang, Ye Wu, Xi-Ru Wu, Netoff Theoden

DOI

2014

[Progress of sudden unexpected death in epilepsy].

Xiao-Juan Tian, Yuehua Zhang

Zhonghua er ke za zhi = Chinese journal of pediatrics

2014

[Study on concordance of ictal and interictal epileptiform activity in patients with tuberous sclerosis complex].

Zhi-Xian Yang, Qing-yan Guo, Jiaxin Zhuang, Xiaoyan Liu, H. Xiong, Ye Wu, Shuang Wang, X. Chang, Yuehua Zhang, X. Bao, Yu-Wu Jiang, J. Qin

Zhonghua er ke za zhi = Chinese journal of pediatrics

DOI

2014

[Efficacy of methylprednisolone therapy for electrical status epilepticus during sleep in children].

Jing Chen, Zhi-xiao Yang, Xiaoyan Liu, Tao-Yun Ji, Na Fu, Ye Wu, H. Xiong, Shuang Wang, X. Chang, Yuehua Zhang, X. Bao, Yu-Wu Jiang, J. Qin

Zhonghua er ke za zhi = Chinese journal of pediatrics

DOI

2014

[Clinical features and PRRT2 mutations in infantile convulsions with paroxysmal choreoathetosis].

Xiao-Ling Yang, Yuehua Zhang, Xiaojing Xu, Shuang Wang, Zhi-Xian Yang, Ye Wu, Xiu-Ju Zhang, Xiaoyan Liu, Xi-Ru Wu

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

DOI

2014

Clinical Diagnosis, Treatment, and ALDH7A1 Mutations in Pyridoxine-Dependent Epilepsy in Three Chinese Infants

Zhi-Xian Yang, Xiao-Ling Yang, Ye Wu, Jing-Min Wang, Yuehua Zhang, H. Xiong, Yu-Wu Jiang, J. Qin

PLoS ONE

DOI

2014

Early clinical features and diagnosis of Dravet syndrome in 138 Chinese patients with SCN1A mutations.

Xiaojing Xu, Yuehua Zhang, Hui-Hui Sun, Xiaoyan Liu, Xiao-Ling Yang, H. Xiong, Yu-Wu Jiang, X. Bao, Shuang Wang, Zhi-Xian Yang, Ye Wu, J. Qin, Qing Lin, Xi-Ru Wu

Brain & development (Tokyo. 1979)

DOI

2014

Postzygotic single-nucleotide mosaicisms in whole-genome sequences of clinically unremarkable individuals

A. Huang, Xiaojing Xu, A. Y. Ye, Qixi Wu, Linlin Yan, Boxun Zhao, Xiaoxu Yang, Yao He, Sheng Wang, Zheng Zhang, B. Gu, Han-Qing Zhao, M. Wang, Hua Gao, Ge Gao, Zhichao Zhang, Xiao-Ling Yang, Xi-Ru Wu, Yuehua Zhang, Li-Ping Wei

Cell Research

DOI

2013

Farmers' demand for weather-based crop insurance contracts: The case of maize in south africa

H. Holly Wang, Raphael N. Karuaihe, Douglas L. Young, Yuehua Zhang

Agrekon，Vol. 520, No. 1

DOI

2013

农产品地理标志品牌化发展研究——以陕西为例

张月花，薛平智

《生产力研究》

2013

我国高新技术产业知识产权能力研究述评

张月花，薛平智，雒媛

《中外企业家》

2013

Clinical analysis of pyridoxine-dependent epilepsy in a child and ALDH7A1 mutation

Zhi-Xian Yang, Xiao-Ling Yang, Jing-Min Wang, Yuehua Zhang, Yu-Wu Jiang

DOI

2013

[Peripheral nervous impairment in a patient with methylmalonic aciduria combined with hyperhomocysteinemia].

Tao-Yun Ji, Yuehua Zhang, Fei-tian Li, J. Qin, Yan-Ling Yang

Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences

2013

Phenotypes and PRRT2 mutations in Chinese families with benign familial infantile epilepsy and infantile convulsions with paroxysmal choreoathetosis

Xiao-Ling Yang, Yuehua Zhang, Xiaojing Xu, Shuang Wang, Zhi-Xian Yang, Ye Wu, Xiaoyan Liu, Xi-Ru Wu

BMC Neurology

DOI

2013

[Clinical and genetic characteristics of glucose transporter type 1 deficiency syndrome].

Yan-yan Liu, X. Bao, Shuang Wang, Na Fu, Xiao-Yan Liu, F. Song, Yan-Ling Yang, Ye Wu, Yuehua Zhang, Jian-Xin Wu, Yu-Wu Jiang, J. Qin, Xi-Ru Wu

Zhonghua er ke za zhi = Chinese journal of pediatrics

DOI

2012

Hog insurance adoption and suppliers' discrimination A bivariate probit model with partial observability

Ying Cao, Yuehua Zhang

China Agricultural Economic Review，Vol. 40, No. 20

DOI

2012

美对华“双反”贸易措施的本质动因与应对策略研究

张月花，张根能，徐瑞平

《生产力研究》

2012

[Genetic and phenotypic characteristics of SCN1A mutations in Dravet syndrome].

Xiaojing Xu, Yuehua Zhang, Hui-Hui Sun, Xiao-Yan Liu, Yu-Wu Jiang, Xi-Ru Wu

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

DOI

2012

Allelic variations of glut-1 deficiency syndrome: the chinese experience.

Yan-yan Liu, X. Bao, Dong Wang, Na Fu, Xiao-Ying Zhang, G. Cao, F. Song, Shuang Wang, Yuehua Zhang, J. Qin, Hong Yang, K. Engelstad, D. De Vivo, Xi-Ru Wu

Pediatric Neurology

DOI

2012

NIPA2 located in 15q11.2 is mutated in patients with childhood absence epilepsy

Yu-Wu Jiang, Yuehua Zhang, Ping-Ping Zhang, T. Sang, Feng Zhang, Tao-Yun Ji, Qiong-Hui Huang, Han Xie, R. Du, Bin Cai, Hai-Juan Zhao, Jing-Min Wang, Ye Wu, Hu-Sheng Wu, Ke-Ming Xu, Xiaoyan Liu, P. Chan, Xi-Ru Wu

Human Genetics

DOI

2012

Niemann-Pick disease type C: analysis of 7 patients

H. Xiong, X. Bao, Yuehua Zhang, You-Gui Xu, J. Qin, Hui-Ping Shi, Xi-Ru Wu

World Journal of Pediatrics

DOI

2012

[Phenotype and SCN1A gene mutation screening in 39 families with generalized epilepsy with febrile seizures plus].

Xiaojing Xu, Yuehua Zhang, Hui-Hui Sun, Xiao-Yan Liu, Hu-Sheng Wu, Xi-Ru Wu

Zhonghua er ke za zhi = Chinese journal of pediatrics

DOI

2012

Genotype/phenotype of 6 Chinese cases with Niemann-Pick disease type C.

H. Xiong, K. Higaki, Cui-Jie Wei, X. Bao, Yuehua Zhang, Na Fu, J. Qin, K. Adachi, Y. Kumura, H. Ninomiya, E. Nanba, Xi-Ru Wu

Gene

DOI

2012

染色体15q11.2和15q13.3区域的微缺失与中国儿童失神癫的相关性

Ping-Ping Zhang, Yuehua Zhang, T. Sang, Feng Zhang, Tao-Yun Ji, Qiong-Hui Huang, Han Xie, Hai-Juan Zhao, Bin Cai, Jing-Min Wang

2012

[Clinical and electroencephalographic characteristics of Jeavons syndrome].

Zhi-Xian Yang, Xiao-Yan Liu, J. Qin, Yuehua Zhang

Zhonghua er ke za zhi = Chinese journal of pediatrics

DOI

2011

The Causes of Epilepsy: Genetic epilepsy with febrile seizures plus

I. Scheffer, Yuehua Zhang

DOI

2011

Childhood absence epilepsy: Elctroclinical features and diagnostic criteria.

Xiu-Wei Ma, Yuehua Zhang, Zhi-Xian Yang, Xiaoyan Liu, Hui-Hui Sun, J. Qin, Xi-Ru Wu, Jian-min Liang

Brain & development (Tokyo. 1979)

DOI

2011

Epilepsy in children with methylmalonic acidemia: electroclinical features and prognosis.

Xiu-Wei Ma, Yuehua Zhang, Yan-Ling Yang, Xiaoyan Liu, Zhi-Xian Yang, X. Bao, J. Qin, Xi-Ru Wu

Brain & development (Tokyo. 1979)

DOI

2011

[Electroclinical features of myoclonic-atonic epilepsy].

Jie Deng, Yuehua Zhang, Xiao-Yan Liu, Zhi-Xian Yang, H. Xiong, Shuang Wang, X. Bao, Yu-Wu Jiang, J. Qin, Qing Lin, Xi-Ru Wu

Zhonghua er ke za zhi = Chinese journal of pediatrics

DOI

2011

[Challenge and tactical solution of off-label using antiepileptic drugs].

Yuehua Zhang

Zhonghua er ke za zhi = Chinese journal of pediatrics

2010

我国企业应诉美国反倾销的特点与问题——基于历年案例的考察

张月花，徐瑞平，张根能

《生产力研究》

2010

Clinical and electrophysiological characteristics of startle epilepsy in childhood.

Zhi-Xian Yang, Xiaoyan Liu, J. Qin, Yuehua Zhang, X. Bao, Shuang Wang, X. Chang

Clinical Neurophysiology

DOI

2010

Genetics of the epilepsies: Genetic twists in the channels and other tales

I. Scheffer, Yuehua Zhang, J. Gécz, L. Dibbens

Epilepsia

DOI

2010

Clinical-electroencephalogram characteristics and its evolutionary process of Dravet syndrome

Xiaoyan Liu, Yuehua Zhang, Hui-Hui Sun, Zhi-Xian Yang, Xiu-Wei Ma

DOI

2010

Analysis of SCN1A mutation and parental origin in patients with Dravet syndrome

Hui-Hui Sun, Yuehua Zhang, Xiaoyan Liu, Xiu-Wei Ma, Zhi-Xian Yang, J. Qin, Yu-Wu Jiang, Yu Qi, Xi-Ru Wu

Journal of Human Genetics

DOI

2010

Generalized epilepsy with febrile seizures plus and classical idiopathic generalized epilepsy

Yuehua Zhang, I. Scheffer

2009

陕西省高技术产业集群效应分析及对策研究

张月花，曹娣，薛伟贤

《中国科技论坛》

2009

[Mutation analysis of the SCN1A gene in severe myoclonic epilepsy of infancy].

Hui-Hui Sun, Yuehua Zhang, Xiaoyan Liu, Xiu-Wei Ma, Hu-Sheng Wu, Ke-Ming Xu, J. Qin, Yu Qi, Xi-Ru Wu

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

DOI

2009

[Clinical and electroencephalographic characteristics of epilepsy with myoclonic absences].

Zhi-Xian Yang, Xiao-Yan Liu, J. Qin, Yuehua Zhang, Ye Wu, Yu-Wu Jiang

Zhonghua er ke za zhi = Chinese journal of pediatrics

2009

Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?

I. Scheffer, Yuehua Zhang, F. Jansen, L. Dibbens

Brain & development (Tokyo. 1979)

DOI

2009

Clinical study and PLA2G6 mutation screening analysis in Chinese patients with infantile neuroaxonal dystrophy

Ye Wu, Yong Jiang, Zhan-Cheng Gao, Ju-li Wang, Yun Yuan, H. Xiong, X. Chang, X. Bao, Yuehua Zhang, Jiang-Xi Xiao, Xi-Ru Wu

European Journal of Neurology

DOI

2009

[Progress in studies on Panayiotopoulos syndrome].

Yuehua Zhang, Xiao-Yan Liu

Zhonghua er ke za zhi = Chinese journal of pediatrics

2009

[Multiplex ligation-dependent probe amplification analysis of subtelomeric chromosome rearrangements in children with idiopathic mental retardation].

Mei-Rong Li, Xiao-zhu Wang, Yan-Ling Yang, Yuehua Zhang, H. Xiong, X. Bao, N. Zhong, Xi-Ru Wu, H. Pan

Zhonghua yi xue za zhi

DOI

2009

A study on epileptic negative myoclonus in atypical benign partial epilepsy of childhood.

Zhi-Xian Yang, Xiaoyan Liu, J. Qin, Yuehua Zhang, X. Bao, X. Chang, Shuang Wang, Ye Wu, H. Xiong

Brain & development (Tokyo. 1979)

DOI

2009

Prospective Study on Ketogenic Diet on Refractory Epilepsy in Children

Yuehua Zhang

2008

陕西优势产业知识产权战略研究

张月花，薛伟贤，薛平智

《中国科技论坛》

2008

陕西省优势产业知识产权发展的思路和对策研究

张月花，薛伟贤，郭永

《西安电子科技大学学报(社会科学版)》

2008

[Congenital muscular dystrophy complicated with tetanized spinal column in a case].

X. Chang, Shu-Hua Chen, Yuehua Zhang

Zhonghua er ke za zhi = Chinese journal of pediatrics

2008

[Clinical diagnosis and therapy of opsoclonus-myoclonus syndrome].

H. Xiong, Jing Peng, Yuehua Zhang, X. Bao, Yu-Wu Jiang, J. Qin

Zhonghua er ke za zhi = Chinese journal of pediatrics

2008

Alpers syndrome with prominent white matter changes.

X. Bao, Ye Wu, L. Wong, Yuehua Zhang, H. Xiong, Ping-Chieh Chou, Cavatina K. Truong, Yu-Wu Jiang, J. Qin, Yun Yuan, Qing Lin, Xi-Ru Wu

Brain & development (Tokyo. 1979)

DOI

2008

Gene symbol: GABRG2. Disease: Generalized epilepsy with febrile seizures plus.

Hui-Hui Sun, Yuehua Zhang, Jian-min Liang, Xiaoyan Liu, Xiu-Wei Ma, Hu-Sheng Wu, Ke-Ming Xu, J. Qin, Yu Qi, Xi-Ru Wu

Human Genetics

2008

Seven novel SCN1A mutations in Chinese patients with severe myoclonic epilepsy of infancy

Hui-Hui Sun, Yuehua Zhang, Jian-min Liang, Xiaoyan Liu, Xiu-Wei Ma, J. Qin, Yu Qi, Xi-Ru Wu

Epilepsia

DOI

2008

Partial Seizures and Atypical Absence Seizures as a Single Ictal Event in a Patient With Lennox-Gastaut Syndrome

Zhi-Xian Yang, Xiaoyan Liu, J. Qin, Yuehua Zhang, X. Bao, H. Xiong

Journal of Child Neurology

DOI

2008

[Progress in molecular genetics in severe myoclonic epilepsy of infancy].

Hui-Hui Sun, Yuehua Zhang

Zhonghua er ke za zhi = Chinese journal of pediatrics

DOI

2008

SCN1A, SCN1B, and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plus

Hui-Hui Sun, Yuehua Zhang, Jian-min Liang, Xiaoyan Liu, Xiu-Wei Ma, Hu-Sheng Wu, Ke-Ming Xu, J. Qin, Yu Qi, Xi-Ru Wu

Journal of Human Genetics

DOI

2008

[Progress in molecular genetics of generalized epilepsy with febrile seizures plus].

Hui-Hui Sun, Yuehua Zhang

Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences

2008

[Clinical and electrophysiologic studies on epileptic negative myoclonus in atypical benign partial epilepsy of childhood].

Zhi-Xian Yang, Xiao-Yan Liu, J. Qin, Yuehua Zhang, X. Bao, X. Chang, Ye Wu, H. Xiong

Zhonghua er ke za zhi = Chinese journal of pediatrics

2007

[Clinical characteristics of cases with leukoencephalopathy with vanishing white matter].

Ye Wu, Yu-Wu Jiang, J. Qin, Jiang-Xi Xiao, Jing-Min Wang, Yan-Ling Yang, Yuehua Zhang, X. Chang, Qing Lin, Xi-Ru Wu

Zhonghua er ke za zhi = Chinese journal of pediatrics

2007

Spinal Cord Demyelination Associated with Biotinidase Deficiency in 3 Chinese Patients

Yan-Ling Yang, Chaoyang Li, Zhao-Yue Qi, Jiang-Xi Xiao, Yao Zhang, S. Yamaguchi, Y. Hasegawa, Y. Tagami, Yu-Wu Jiang, H. Xiong, Yuehua Zhang, J. Qin, Xi-Ru Wu

Journal of Child Neurology

DOI

2007

[Clinical characteristics and treatment of Rasmussen syndrome in 16 children].

Yuehua Zhang, Li-hua Pu, X. Liu, H. Xiong, Yun-Lin Li, Xing-Zhou Liu, G. Luan, J. Qin, Xi-Ru Wu

Zhonghua er ke za zhi = Chinese journal of pediatrics

2007

[Clinical and genetic analysis of a family with Pelizaeus-Merzbacher disease].

Hui-Fang Wang, Ye Wu, Yu-Wu Jiang, Jing-Min Wang, M. Tang, Yuehua Zhang, J. Qin, Qing Lin, Xi-Ru Wu

Zhonghua er ke za zhi = Chinese journal of pediatrics

2007

[Clinical studies on fifty-seven Chinese patients with combined methylmalonic aciduria and homocysteinemia].

Yao Zhang, Jinqing Song, Ping Liu, Rong Yan, Jin-Hua Dong, Yan-Ling Yang, Lan Wang, Yu-Wu Jiang, Yuehua Zhang, J. Qin, Xi-Ru Wu

Zhonghua er ke za zhi = Chinese journal of pediatrics

2007

[Prenatal diagnosis of X-linked adrenoleukodystrophy].

X. Bao, L. Ping, Ai-hua Wang, H. Pan, Ye Wu, H. Xiong, Yuehua Zhang, Chun-yan Shi, J. Qin, Xi-Ru Wu

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

2006

[Diagnostic value of muscle, sural nerve and skin biopsies in childhood neuromuscular disorders].

X. Chang, Jia-Yun Zhou, Yun Yuan, Ye Wu, Yue-Xing Li, Wei Zhang, Yu-Wu Jiang, X. Bao, Yuehua Zhang, Shuang Wang, H. Xiong, Yan-Ling Yang, J. Qin

Zhonghua er ke za zhi = Chinese journal of pediatrics

DOI

2006

New variants in the CACNA1H gene identified in childhood absence epilepsy.

Jian-min Liang, Yuehua Zhang, Ju-li Wang, H. Pan, Hu-Sheng Wu, Ke-Ming Xu, Xiaoyan Liu, Yu-Wu Jiang, Yan Shen, Xi-Ru Wu

Neuroscience Letters

DOI

2006

Acute metabolic crisis induced by vaccination in seven Chinese patients.

Yan-Ling Yang, S. Suján, Fang Sun, Yuehua Zhang, Yu-Wu Jiang, Jinqing Song, J. Qin, Xi-Ru Wu

Pediatric Neurology

DOI

2006

[Clinical characteristics and long-term prognosis of Landau-Kleffner syndrome].

Shuang Wang, Yuehua Zhang, X. Bao, Ye Wu, Yu-Wu Jiang, Xiao-Yan Liu, J. Qin

Zhonghua er ke za zhi = Chinese journal of pediatrics

DOI

2006

[Research on genes susceptible to childhood absence epilepsy].

Jian-min Liang, Yuehua Zhang, Xi-Ru Wu

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

2006

The genotype and phenotype studies of 40 Chinese patients with X-linked adrenoleukodystrophy (X-ALD).

L. Ping, X. Bao, Ai-hua Wang, H. Pan, Ye Wu, H. Xiong, Yuehua Zhang, Yu-Wu Jiang, J. Qin, Xi-Ru Wu

Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences

2006

[The effect of CACNA1H gene G773D mutation on calcium channel function].

Ju-li Wang, Chong-yang Han, Yuxiao Jing, Yu-Cai Chen, Nan Feng, Jian-Jun Lu, Yuehua Zhang, H. Pan, Hu-Sheng Wu, Ke-Ming Xu, Yu-Wu Jiang, Jian-min Liang, Ling Wang, Xiao-liang Wang, Yan Shen, Xi-Ru Wu

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

2006

Clinical and Biochemical Studies on Chinese Patients With Methylmalonic Aciduria

Yan-Ling Yang, Fang Sun, Jinqing Song, Y. Hasegawa, S. Yamaguchi, Yuehua Zhang, Yu-Wu Jiang, J. Qin, Xi-Ru Wu

Journal of Child Neurology

DOI

2006

CACNA1I is not associated with childhood absence epilepsy in the Chinese Han population.

Ju-li Wang, Yuehua Zhang, Jian-min Liang, H. Pan, Hu-Sheng Wu, Ke-Ming Xu, Xiaoyan Liu, Yu-Wu Jiang, Yan Shen, Xi-Ru Wu

Pediatric Neurology

DOI

2006

[Diagnosis of congenital muscular dystrophy and clinical significance of merosin expression].

H. Xiong, S. Yao, Yun Yuan, X. Chang, Ye Wu, X. Bao, Yuehua Zhang, Hu-Sheng Wu, Lin Chen, J. Qin, Xi-Ru Wu

Zhonghua er ke za zhi = Chinese journal of pediatrics

DOI

2005

[T-type calcium channel gene-CACNA1H is a susceptibility gene to childhood absence epilepsy].

Jian-Jun Lu, Yuehua Zhang, Yu-Cai Chen, H. Pan, Ju-li Wang, Lei Zhang, Hu-Sheng Wu, Ke-Ming Xu, Xiao-Yan Liu, La-Di Tao, Yan Shen, Xi-Ru Wu

Zhonghua er ke za zhi = Chinese journal of pediatrics

2005

[Clinical and laboratory screening studies on urea cycle defects].

Yan-Ling Yang, Fang Sun, N. Qian, Jinqing Song, Shuang Wang, X. Chang, Hong-Yun Yang, Shu-Qin Wang, Long-ming Li, Yuehua Zhang, X. Bao, Ming Li, Yu Qi, J. Qin, Xi-Ru Wu

Zhonghua er ke za zhi = Chinese journal of pediatrics

2005

[Advances of research in ion channels in idiopathic epilepsy].

Ju-li Wang, Yuehua Zhang, Xi-Ru Wu

Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences

2005

离子通道与特发性癫(疒间)研究进展

Ju-li Wang, Yuehua Zhang, Xi-Ru Wu

2005

[Screening for carrier and prenatal diagnosis of X-linked adrenoleukodystrophy].

Ai-hua Wang, X. Bao, H. Xiong, H. Pan, Ye Wu, Yuehua Zhang, Chun-yan Shi, J. Qin, Xi-Ru Wu

Zhonghua er ke za zhi = Chinese journal of pediatrics

2005

ABCD1 gene mutations in Chinese patients with X-linked adrenoleukodystrophy.

H. Pan, H. Xiong, Ye Wu, Yuehua Zhang, X. Bao, Yu-Wu Jiang, Xi-Ru Wu

Pediatric Neurology

DOI

2004

[Calcium channels and human genetic diseases].

Yuehua Zhang, Xi-Ru Wu

Zhonghua er ke za zhi = Chinese journal of pediatrics

2004

Case-control study and transmission/disequilibrium tests of the genes encoding GABRA5 and GABRB3 in a Chinese population affected by childhood absence epilepsy.

Jian-Jun Lu, Yuehua Zhang, H. Pan, Yu-Cai Chen, Xiao-Yan Liu, Yu-Wu Jiang, X. Bao, Yan Shen, Hu-Sheng Wu, Ke-Ming Xu, Xi-Ru Wu

Chinese Medical Journal

2004

[X-linked adrenoleukodystrophy ABCD1 gene mutation analysis in China].

H. Pan, H. Xiong, Yuehua Zhang, Ye Wu, X. Bao, Yu-Wu Jiang, Xi-Ru Wu

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

会议论文

2013

科技型小微企业知识产权能力建设研究

张月花，薛平智，储有捷

《科技型小微企业创新发展论坛》

此主页由公开资料整理，尚未经学者本人认领。